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Understanding phase-transfer catalytic synthesis of fullerenol and its interference from carbon dioxide and ozone
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Metadata
Document Title
Understanding phase-transfer catalytic synthesis of fullerenol and its interference from carbon dioxide and ozone
Author
Chokaouychai S., Zhang Q.
Name from Authors Collection
Affiliations
School of Aerospace, Transport and Manufacturing (SATM), Cranfield University, Cranfield, Bedfordshire, MK43 0AL, United Kingdom; National Science and Technology Development Agency (NSTDA), Thailand Science Park, 111 Phahonyothin Road, Khlong Nueng, Khlong Luang, Pathum Thani 12120, Thailand; BCMaterials, Basque Center for Materials, Applications and Nanostructures, UPV/EHU Science Park, Leioa, 48940, Spain; IKERBASQUE, Basque Foundation for Science, Bilbao, 48013, Spain
Type
Article
Source Title
Research on Chemical Intermediates
ISSN
09226168
Year
2020
Volume
46
Issue
12
Page
5391-5415
Open Access
Hybrid Gold, Green
Publisher
Springer Science and Business Media B.V.
DOI
10.1007/s11164-020-04269-7
Abstract
Phase-transfer catalytic reaction involving the use of tetrabutylammonium hydroxide (TBAH) as catalyst and sodium hydroxide (NaOH) solution as the source of hydroxide ions is among the popular choices for synthesis of fullerenol, the polyhydroxylated fullerene. To further understand the process, two experiments were conducted to preliminarily explore the influences of the amount of TBAH and NaOH, respectively, in terms of the achieved level of hydroxylation (i.e. number of hydroxyl groups per fullerenol molecule). The process responded to the variation of the amount of TBAH (over a twofold series of 3–192 drops, average volume 0.0223 ± 0.0004 ml per drop) in a nonlinear manner with a local maximum achieved from 24 drops TBAH (giving 13 OH groups) and a local minimum from 48 drops (giving 8 groups). To the variation of the amount of NaOH (over the range of 0.5–8.0 ml NaOH), the fitted function of the process response resembled Freundlich adsorption isotherm, with an initially increasing trend before levelling off at 4.0 ml NaOH (giving 15 OH groups). It is therefore suggested that fullerene hydroxylation could be explained by liquid–solid adsorption. In addition, it was found that ambient carbon dioxide led to the existence of sodium carbonate in the bulk of the collected product (although not chemically bound). It was also discovered that ambient ozone adversely affected fullerenol synthesis by converting C60 fullerene into fullerene epoxide (C60O). The affected syntheses thus produced epoxide-containing fullerenol instead. © 2020, The Author(s).
Keyword
Carbon dioxide | Carbon nanomaterials | Fullerene epoxide | Fullerenol | Ozone | TBAH
Funding Sponsor
National Institute of Advanced Industrial Science and Technology
License
CC BY
Rights
Author
Publication Source
Scopus